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Autoimmune polyendocrinopathy syndrome, type 1

Known as: Autoimmune polyendocrine syndrome, type 1, Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), Hypoadrenocorticism with hypoparathyroidism and superficial moniliasis 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (1)

Polyendocrinopathies, Autoimmune
Polyglandular Deficiency Syndrome, Persian-Jewish TypePolyglandular Type I Autoimmune Syndrome

Papers overview

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2017
2017
Clonal Analysis of Regulatory T Cell Defect in Patients with Autoimmune Polyendocrine Syndrome Type 1 Suggests Intrathymic Impairment
Mutations in the autoimmune regulator gene disrupt thymic T cell development and negative selection, leading to the recessively… 
2017
2017
Inborn errors of T cell immunity underlying autoimmune diseases
AbstractImmunopathological diseases have traditionally been classified as autoimmune/inflammatory, allergic, and primary… 
2017
2017
Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1
Abstract Autoimmune polyendocrine syndrome type 1 (APS1) is a rare monogenic autoimmune disorder caused by mutations in the… 
2014
2014
Gonadal function in males with autoimmune Addison's disease and autoantibodies to steroidogenic enzymes
Steroidogenic enzyme autoantibodies (SEAbs) are frequently present and are markers of autoimmune premature ovarian failure (POF… 
2013
2013
Autoantibodies against aromatic amino acid hydroxylases in patients with autoimmune polyendocrine syndrome type 1 target multiple antigenic determinants and reveal regulatory regions crucial for…
2012
2012
Novel neuronal and endocrine autoantibody targets in autoimmune polyendocrine syndrome type 1
Context. Although pituitary autoantibodies have frequently been reported in Autoimmune Polyendocrine Syndrome type 1 (APS1), the… 
2011
2011
Autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy in Calabria: Clinical, immunological and genetic patterns
Autoimmune polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED), also known as autoimmune polyendocrine syndrome type 1… 
2008
2008
An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune…
An 8-year-old boy presented in 1995 with a 2-year history of hypertransaminasemia and hypergammaglobulinemia. Afterwards the… 
2000
2000
“Vascular profiles” of regenerative and dysplastic nodules
Review
1997
Review
1997
Recent developments in autoimmune liver diseases
Several diseases are regarded as autoimmune liver diseases. Apart from the cholestatic liver diseases, primary biliary cirrhosis… 
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